34 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SMART READ BIOLOGICAL TEST PACK
FDA 510(k)
FDA Class 2
·General Hospital
PIPELLE®
FDA UDI
LABORATOIRE CCD·03700111400719·Device for endometrial sampling
SAV
FDA UDI
Diversified Products, Inc.·00037741210399·
GEN4 INTERACTIVE
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828195287·
Electro Lavage
FDA UDI
MECTRA LABS, INC.·00817984010433·Electro Lavage Spatula Double Bottle
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04019702275704·Elvarex 3/Thigh High/Profile, Slant, Open Toe, ...
OsteoMed
FDA UDI
OSTEOMED LLC·00845694043311·2.0mm, 7 Hole Curved Plate with Screws, Sterile
Minuteman G5
FDA UDI
Spinal Simplicity, LLC·M9431001030000·Minuteman G5 MIS Fusion Plate
EARLE'S BALANCED SALT SOLUTION (EBSS) NO. 210-3000
FDA 510(k)
FDA Class 1
·Hematology
ROD, FIXATION, INTRAMEDULLARY
FDA Adverse Event
Injury
·SYNTHES USA·Product code HSB·August 9, 2016
GRAMS NYLON NONABSORBABLE SUTURE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MEDTRONIC INVISX BURR HOLE LOCK, MODEL 60520
FDA 510(k)
FDA Class 2
·Neurology
STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN SYMPTOMS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code NHL·June 28, 2024
TENSION FREE VAGINAL TAPE
FDA Adverse Event
Injury
·ETHICON, INC.·Product code OTN·May 9, 2013
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·September 19, 2014
INTEGRITY RX CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MAF·May 5, 2011
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·November 13, 2014
MINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·September 15, 2025
ROD, FIXATION, INTRAMEDULLARY
FDA Adverse Event
Injury
·SYNTHES USA·Product code HSB·July 25, 2016
SINGLE SHOT EPIDURAL ANESTHESIA KIT/Product SKU's (Codes) AK-03000, AM-03000, BH-03000, DH-03000, KC-03000, SA-03001 and SH-03001. Epidural Anesthesia Kit
FDA Recall
Terminated
·Arrow International Inc·Product code CAZ·October 29, 2010